Hypericum patulum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Hypericum patulum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Internal ID UUID644021661d416476678396
Scientific name Hypericum patulum
Authority Thunb.
First published in Syst. Veg. ed. 14 : 700 (1784)

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Synonyms Top

Scientific name Authority First published in
Komana patula (Thunb.) Y.Kimura Nom. Pl. Jap. : 509 (1939)
Norysca patula (Thunb.) Voigt Hort. Suburb. Calcutt. : 90 (1845)
Eremanthe patula (Thunb.) K.Koch Hort. Dendrol. : 65 (1853)
Hypericum argyi H.Lév. & Vaniot Bull. Soc. Bot. France 54: 591 (1908)
Hypericum hookerianum var. dentatum S.N.Biswas Bull. Bot. Surv. India 25(1-4): 195. 1985 [1983 publ. 1985]

Common names Top

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Language Common/alternative name
French millepertuis doré
Upper Sorbian Šěroki zahrodny křižomnik
Japanese きんしばい
Japanese キンシバイ
Polish dziurawiec rozpierzchły
Chinese 金丝桃
Chinese 黄花香
Chinese 芒种花
Chinese 芒種花
Chinese 金丝梅
Chinese 金絲梅
Chinese 雲南連翹

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000728083
USDA Plants HYPA12
Tropicos 7800880
KEW urn:lsid:ipni.org:names:927423-1
The Plant List kew-2858661
Open Tree Of Life 521125
NCBI Taxonomy 212239
IPNI 927423-1
iNaturalist 349201
GBIF 3713491
EPPO HYPPT
EOL 2889790
USDA GRIN 19598
Wikipedia Hypericum_patulum

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
A Network Pharmacology and Molecular Dynamics Simulation-Based Study of Qing Run Hua Jie Decoction in Interstitial Pneumonia Treatment Li C, Lian Y, Lin Y, Li Z Infect Drug Resist 16-Feb-2024
PMCID:PMC10878319
doi:10.2147/IDR.S433755
PMID:38379588
Mukaiyama aldol reaction: an effective asymmetric approach to access chiral natural products and their derivatives/analogues Mushtaq A, Zahoor AF RSC Adv 08-Nov-2023
PMCID:PMC10631541
doi:10.1039/d3ra05058k
PMID:38025859
Taxonomy and Multigene Phylogeny of Diaporthales in Guizhou Province, China Wang SY, McKenzie EH, Phillips AJ, Li Y, Wang Y J Fungi (Basel) 15-Dec-2022
PMCID:PMC9785342
doi:10.3390/jof8121301
PMID:36547633
Advancements and future prospective of DNA barcodes in the herbal drug industry Mahima K, Sunil Kumar KN, Rakhesh KV, Rajeswaran PS, Sharma A, Sathishkumar R Front Pharmacol 21-Oct-2022
PMCID:PMC9635000
doi:10.3389/fphar.2022.947512
PMID:36339543
Dearomative gem-diprenylation of hydroxynaphthalenes by an engineered fungal prenyltransferase Xu Y, Li D, Wang W, Xu K, Tan G, Li J, Li SM, Yu X RSC Adv 27-Sep-2022
PMCID:PMC9514087
doi:10.1039/d2ra04837j
PMID:36276050
Hyperoside as a Potential Natural Product Targeting Oxidative Stress in Liver Diseases Jang E Antioxidants (Basel) 25-Jul-2022
PMCID:PMC9331122
doi:10.3390/antiox11081437
PMID:35892639
A study of the plant folk nomenclature of the Yi people in Xiaoliangshan, Yunnan Province, China, and the implications for protecting biodiversity Addi YW, Zhang Y, Ding XY, Guo CA, Wang YH J Ethnobiol Ethnomed 15-Mar-2022
PMCID:PMC8925061
doi:10.1186/s13002-022-00504-0
PMID:35292043
The application of mass spectrometry imaging in traditional Chinese medicine: a review Huang L, Nie L, Dai Z, Dong J, Jia X, Yang X, Yao L, Ma SC Chin Med 05-Mar-2022
PMCID:PMC8898510
doi:10.1186/s13020-022-00586-8
PMID:35248086
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Herbal plants traded at the Kaili medicinal market, Guizhou, China Liu S, Zhang B, Zhou J, Lei Q, Fang Q, Kennelly EJ, Long C J Ethnobiol Ethnomed 29-Nov-2021
PMCID:PMC8628420
doi:10.1186/s13002-021-00495-4
PMID:34844607
Xanthone Glucosides: Isolation, Bioactivity and Synthesis Huang Q, Wang Y, Wu H, Yuan M, Zheng C, Xu H Molecules 14-Sep-2021
PMCID:PMC8465223
doi:10.3390/molecules26185575
PMID:34577044
Taxonomical re-examination of the genus Neofusicoccum in Japan Hattori Y, Ando Y, Nakashima C Mycoscience 20-Jul-2021
PMCID:PMC9721510
doi:10.47371/mycosci.2021.03.008
PMID:37092171
Meroterpenoids: A Comprehensive Update Insight on Structural Diversity and Biology Nazir M, Saleem M, Tousif MI, Anwar MA, Surup F, Ali I, Wang D, Mamadalieva NZ, Alshammari E, Ashour ML, Ashour AM, Ahmed I, E, Green IR, Hussain H Biomolecules 29-Jun-2021
PMCID:PMC8301922
doi:10.3390/biom11070957
PMID:34209734
Microbial soluble aromatic prenyltransferases for engineered biosynthesis Chen HP, Abe I Synth Syst Biotechnol 15-Mar-2021
PMCID:PMC7973389
doi:10.1016/j.synbio.2021.02.001
PMID:33778178
Characteristic metabolites of Hypericum plants: their chemical structures and biological activities Tanaka N, Kashiwada Y J Nat Med 08-Feb-2021
PMCID:PMC8159811
doi:10.1007/s11418-021-01489-y
PMID:33555487

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzophenones
[3-(2,2-Dimethyl-4-prop-1-en-2-ylcyclopentyl)-2,4,6-trihydroxyphenyl]-phenylmethanone 162877970 Click to see CC(=C)C1CC(C(C1)(C)C)C2=C(C(=C(C=C2O)O)C(=O)C3=CC=CC=C3)O 366.40 unknown https://doi.org/10.1016/S0031-9422(98)80068-X
[3-[(1R,4R)-2,2-dimethyl-4-prop-1-en-2-ylcyclopentyl]-2,4,6-trihydroxyphenyl]-phenylmethanone 162877971 Click to see CC(=C)C1CC(C(C1)(C)C)C2=C(C(=C(C=C2O)O)C(=O)C3=CC=CC=C3)O 366.40 unknown https://doi.org/10.1016/S0031-9422(98)80068-X
[3-[(1S,4S)-2,2-dimethyl-4-prop-1-en-2-ylcyclopentyl]-2,4,6-trihydroxyphenyl]-phenylmethanone 12147115 Click to see CC(=C)C1CC(C(C1)(C)C)C2=C(C(=C(C=C2O)O)C(=O)C3=CC=CC=C3)O 366.40 unknown https://doi.org/10.1016/S0031-9422(98)80068-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(98)80068-X
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.3109/13880209109082884
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(98)80068-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(98)80068-X
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(98)80068-X
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(98)80068-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,5,6-Tetrahydroxyxanthone 5479774 Click to see C1=CC(=C(C2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)O 260.20 unknown https://doi.org/10.1016/S0031-9422(96)00651-6
1,3,7-Trihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 5858087 Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 422.30 unknown https://doi.org/10.1016/0031-9422(95)00882-9
1,5,6-trihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 162872254 Click to see C1=CC(=C(C2=C1C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 422.30 unknown https://doi.org/10.1021/NP980519X
1,5,6-trihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 53883544 Click to see C1=CC(=C(C2=C1C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 422.30 unknown https://doi.org/10.1021/NP980519X
1,5,6-Trihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 162872253 Click to see C1=CC(=C(C2=C1C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 422.30 unknown https://doi.org/10.1021/NP980519X
2-(2,2-Dimethyl-4-prop-1-en-2-ylcyclopentyl)-1,3,5,6-tetrahydroxyxanthen-9-one 10408433 Click to see CC(=C)C1CC(C(C1)(C)C)C2=C(C3=C(C=C2O)OC4=C(C3=O)C=CC(=C4O)O)O 396.40 unknown https://doi.org/10.1016/0031-9422(95)00882-9
2-(2,2-Dimethyl-4-prop-1-en-2-ylcyclopentyl)-1,3,6-trihydroxy-5-methoxyxanthen-9-one 77916194 Click to see CC(=C)C1CC(C(C1)(C)C)C2=C(C3=C(C=C2O)OC4=C(C3=O)C=CC(=C4OC)O)O 410.50 unknown https://doi.org/10.1016/0031-9422(95)00080-Q
https://doi.org/10.1016/J.PHYTOCHEM.2008.10.016
2-[(1R,4R)-2,2-dimethyl-4-prop-1-en-2-ylcyclopentyl]-1,3,5,6-tetrahydroxyxanthen-9-one 162854822 Click to see CC(=C)C1CC(C(C1)(C)C)C2=C(C3=C(C=C2O)OC4=C(C3=O)C=CC(=C4O)O)O 396.40 unknown https://doi.org/10.1016/0031-9422(95)00882-9
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,5,6-trihydroxyxanthen-9-one 54276319 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC5=C(C4=O)C=CC(=C5O)O)O)CO)O)O)O)O)O 568.50 unknown https://doi.org/10.1021/NP980519X
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1,5,6-trihydroxyxanthen-9-one 162961321 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC5=C(C4=O)C=CC(=C5O)O)O)CO)O)O)O)O)O 568.50 unknown https://doi.org/10.1021/NP980519X
Patulone 136803273 Click to see CC(=CCC1(C2=C(C=C(C1=O)O)OC3=CC(=CC(=C3C2=O)O)O)CC=C(C)C)C 396.40 unknown https://doi.org/10.1016/S0031-9422(96)00651-6
Paxanthonin 70698384 Click to see CC(=C)C1CC(C(C1)(C)C)C2=C(C3=C(C=C2O)OC4=C(C3=O)C=CC(=C4OC)O)O 410.50 unknown https://doi.org/10.1016/0031-9422(95)00080-Q
Tripteroside 5281664 Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 422.30 unknown https://doi.org/10.1016/0031-9422(95)00882-9
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,3,6-Trihydroxy-5-methoxy-2-prenylxanthone 14886043 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC(=C3OC)O)O)C 342.30 unknown https://doi.org/10.1016/0031-9422(95)00080-Q
garcinone B 5495928 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(C=C4)(C)C)O)C 394.40 unknown https://doi.org/10.1016/J.NEULET.2005.10.023
https://doi.org/10.1016/0031-9422(94)00664-F
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
5,9,11-Trihydroxy-3,3-dimethyl-8-(3-methyl-2-butenyl) pyrano[3,2-a]xanthen-12(3h)-one 101920414 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C=C(C4=C3C=CC(O4)(C)C)O)C 394.40 unknown https://doi.org/10.1016/0031-9422(94)00664-F
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
1,3,6,7-Tetrahydroxy-8-prenylxanthone 15307924 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)O)C 328.30 unknown https://doi.org/10.1016/0031-9422(94)00664-F
gamma-Mangostin 5464078 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)O)CC=C(C)C)O)C 396.40 unknown https://doi.org/10.1016/0031-9422(93)85286-Z
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
Paxanthone 71591732 Click to see CC1(C=CC2=C3C(=CC(=C2O1)OC)OC4=CC(=CC(=C4C3=O)O)O)C 340.30 unknown https://doi.org/10.1016/0031-9422(93)85286-Z
toxyloxanthone B 14886044 Click to see CC1(C=CC2=C(O1)C(=CC3=C2C(=O)C4=C(C=C(C=C4O3)O)O)O)C 326.30 unknown https://doi.org/10.3109/13880209109082884
https://doi.org/10.1016/0031-9422(93)85286-Z
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(96)00651-6
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(96)00651-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.3109/13880209109082884
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astilbin 119258 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 unknown https://doi.org/10.3109/13880209109082884
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.3109/13880209109082884

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